Enrollment Deadline: 1 November 2026

Participants will analyze a single human blood sample for Single Nucleotide Polymorphism (SNP) markers using specialized SNP genotyping platforms to generate a SNP profile and upload their data for comparison to consensus data provided by ForenSeq Kintelligence. Data from any SNP technology will be accepted and compared to consensus data, which is currently derived from the marker sets provided by the platform ForenSeq Kintelligence.

Sample Description: Choose between blood on an FTA™ Micro Card (Test 5911) or two Swabs (Test 5912). The genomic material provided in Tests 5911 and 5912 are sourced from the same donor and shipped at the same time, and reporting aspects are combined. A different donor source is used for Tests 5915/5916.

Samples ship in April.

Additional Information: SNP data should be based on human genome build hg 38; if you are unsure whether your kit uses this build, please contact CTS. Current acceptable SNP data formats include .txt, .csv, and .vcf. If your results are produced in another format, please contact CTS.

This test is included on CTS' Scope of Accreditation to ISO/IEC 17043.